Комментарии:
Thank you very much.
ОтветитьIn case of AAS atomic absorption spectroscopy
The linearity start from 0.1 ppm to 0.5 ppm (LOD)
and the concentration fall below the 0.1 i.e 0.023 then
What will be the result?
Should we calculate this or not
If not then what will be the result?
If anyone have answer
Plz let me know
Hi sir
Why In visual observation LOQ not determined .
Ple send the answer
Hello Sir I got confused with how to compute the residuals especially the predictable response which you mentioned (mx + c). Kindly explain in detailed. And thank you in advance if you will notice my comment and query.
ОтветитьWhy the number 3 comes in the formula for LOD?
ОтветитьThank you👏🏼👏🏼👏🏼
ОтветитьHello sir... according to ich guidelines loq value considered maximum 50% of our spec limit if our loq not stablish 50% or below spec limit than what will be do...??
Please suggest me sir...and explain what is the reason not stablish loq below 50%..
Great efforts
ОтветитьWhat if the specification limit is below to the quantification limit then is that LOQ is valid?
ОтветитьIs there need of seprate calibration curves for QL and DL.
ОтветитьIt was very informative & useful information and you explained ina detail so anyone can understand, Great ..Help
ОтветитьHighly informative sir 👍🙏
ОтветитьSuper sir
ОтветитьTanks
Ответитьhi Can you explain more about how to ca the calculate the residuals, I'm confused about the formula
ОтветитьSir what is maximum limit of impurity
ОтветитьYou made video on related substances
ОтветитьTQ Sir..
Ответитьcan we get the PPT PDF plz
ОтветитьSend me excel sheet sir plz.
ОтветитьThank you so much sir
ОтветитьGreat sir,your explanation is very versatile 👌, useful for us.
ОтветитьVery Informative lecture😍
ОтветитьSeperate curve for detection limit in that LOQ should not be added other linearity level can be added. Is it so
ОтветитьActual value and predictable value explain with another one more example in visible manner
Ответить10.35 minutes can u explain a little elaborate with other example
ОтветитьSir ur expalnation is very good but ihave a one doubt for blank mesurement method
1. We are inject blank solution or placebo 60 mesurements but the solutions not present in our analyte then how integrate peak and caliculate sddeviation
Your explanation is very powerful and easily understand by anyone. Appreciate.
ОтветитьThank you sir, Highly informative. Please put video for gradient method development in HPLC
ОтветитьWhy we determined lod and loq??
ОтветитьSir please make a vidio in hindi language for better understanding.then will be more grow your channel and views and gain subscribers.
ОтветитьSir please made a video for set the LOQ limit for 2 to 5 impurity present in sample having different uv
Please made all clear about the method validation with the example it will be helpful for us
ur explanation was amazing and crystal clear, keep making the lectures to enrich knowledge
ОтветитьVery helpful sir, can we have a video about impurity method validation from protocol preparation to report generation?
ОтветитьWhich concentrations need to be selected while determine the lod and loq?can we go below 1 ppm too in the given example...
Ответитьcan i get it in pdf
Ответить